articulo 001

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A. G. Pinkus Baylor University Waco, Texas 76703 Magnesocene: Structure and Bonding Covalent or ionic? Although the most common state of coordination for mag- nesium in its compounds is four (1), examples of three-(2), five-(3), six-(4), and eight-coordination (5) have also been reported. An unusual type of bonding for magnesium which does not fit into any of these categories occurs in magneso- cene. 1 Magnesocene is a member of the general class of or- ganometallic compounds known as metallocenes (6) or "sandwich" compounds of which the first example to be rec- ognized is the well-known ferrocene. Although it is generally agreed that bonding in metallocenes of transition metáis ap- pears to be predominantly covalent, the nature of bonding in magnesocene is currently in dispute. This paper will present a bríef review of the structures and bonding proposed for magnesocene leading u p t o the most recent work. Although magnesocene was first prepared (7) by addition of cyclopentadiene to ethylmagnesium bromide and removing ether solvent in vacuo, it can also be prepared (8) by the re- action of metallic magnesium with cyclopentadiene (eqn. (D). 2C 6 H 6 + Mg - H 2 + Mg(C 5 H 5 ) 2 (1) Magnesocene is a useful intermedíate for the preparation (9) of other metallocenes either in the molten state or in solution (eqn. (2)). The high free energy of formation of MgCl2 favors the metathesis. Mg(C 5 H 5 )2 + MC1 2 - M(C 5 H 5 ) 2 + MgCl 2 (2) Magnesocene has been reported (10) to have been prepared in a rose-colored modification in addition to the better-known form. Weiss and Fisher (11) determined that Mg(C 5 H 5 ) 2 i n t h e crystalline state had a sandwich-like structure and proposed weak covalent d 2 sp 3 hybridization overlapping the ionic electrostatic binding between the metal and cyclopentadienyl ions. Based on magnetic, spectral, and chemical investigations, Wilkinson, Cotton, and Birmingham (12) concluded that ionic bonding was present; the two cyclopentadienide anions would be expected on electrostatic grounds to align themselves on opposite sides of the catión with parallel planes and to very closely resemble ferrocene. The concept of ionic bonding in Mg(CsH 5 )2 was further elaborated by Cotton and Reynolds (13). Lippincott, Xavier, and Steele (14) studied the infrared and Raman spectra of solutions and the solid state and in comparison with studies on ferrocene confirmed the sand- wich-type structure. However, they concluded that their re- sults were not in agreement with the ionic bonding concept but were better explained by covalent ring-to-metal bonding which was, however, weaker than the metal-to-ring bonding in ferrocene. From a gas-phase electrón diffraction study, Haaland, et al. (15,16), determined that the best agreement between calculated and experimental intensities was obtained by assuming eclipsed C5H5 rings (Dñrt symmetry) (see figure). However, a model with staggered symmetry (Z) 5( ¿) could not T 2.008» 1.423A Structure of magnesocene ( 15, 16). si de view (rings perpendicular) be conclusively ruled out. They also concluded that there was no significant deviation from planarity for the C5H5 rings and that magnesocene is best regarded as a covalent rather than an ionic compound. More recently, Aleksanyan and coworkers (17) obtained Raman and infrared spectra on the compound. Raman results were for solid and melt forms and included depolarization measurements while infrared data for the solid covered the range 400-3200 cm - 1 . Their analysis of the data led to the conclusión that the Mg-Cp bond is mainly ionic. Literature Cited (1) Bailar, J. C, Jr. in "The Chemistry of the Coordination Compounds," (Editor: Bailar, J. C, Jr.), Reinhold, New York, 1956, p. 243. (2) For a recent review: Pinkus, A. G., Coord. Chem. Rev., 25, 173 (1978). (3) Stucky, G., and Rundle, R. E., J. Amer. Chem. Soc, 86, 4821 (1964); Vallino, M., Or- ganometal. Chem., 20, 1 (1969). (4) Schroder, F., and Spandau, H., Naturwissenschaften, 53, 360 (1966); Schróder, F. A., Chem. Ber., 102, 2035 (1969); Atwood, J. L., and Stuckey, G. D., J. Organometal. Chem., 13, 53 (1968); Toney, J. D., and Stucky, G. D., J. Organometal Chem., 28, 5(1971). (5) Shannon, R. D., and Prewitt, C. T., Acta Cryst., B25,925 (1969); Mortier, W. J., Pluth, J. J., and Smith, J. B., Nature, 256, 718 (1975). (6) Reviews dealing in part with various aspects of metallocenes (excluding ferrocenes): (a) Pauson, P. L., " Cyclopentadienyl Metal Compounds" in "Organometallic Chemistry", (Editor: Zeiss, H.), Reinhold, New York, 1960, Chap. 7, pp. 346-379; (b) Zeiss, H., "Arene Complexes of the Transition Metals" in ibid., Chap. 8, pp. 380-425. (c) Birmingham, C. M-, "Synthesis of Cyclopentadienyl Metal Compounds," in "Advances in Organometallic Chemistry," Vol. 2, (Editors: Stone, F. G. A., and West, R.) Academic Press, New York, 1964, pp. 365-413; (d) Churchill, M . R., and Masón, R., "The Structural Chemistry of Organo-Transition Metal Complexes: Some Recent Developments," ibid., vol. 5, 1967, pp. 93-135; (e) Cais, M., and Lupin, M. S., "Mass Spectra of Metallocenes & Related Compounds," ibid., vol. 8, 1970, pp. 211-333; (f) Slocum, D. W., and Ernst, C. R., "Electronic Effects in Metallocenes and Certain Related Systems," ibid., vol. 10, 1972, pp. 79-114; (g) Bruce, M. I., "Organo-Transition Metal Chemistry-A Guide to the Literature 1950-1970," ibid., vol. 10, pp. 273-346; (h) Rubezhov, A. Z. and Gubin, S. P., "Ligand Substitution in Transition Metal x-Complexes," ibid., vol. 10, pp. 347-417; (i) Bruce, M. I., "The Literature of Organo-Transition Metal Chemistry 1971," ibid., vol. 11,1973, pp. 447 ff; (j) Bruce, M. I., "The Literature of Organo Transition Metal Chemistry 1972," ibid., vol. 12, 1974, pp. 379-407; (k) Silverthorn, W. E., "Arene Transition Metal Chemistry," ibid., vol. 13, 1975, pp. 47-137; (1) Razuvaev, G. A., and Latyaeva, V. N., "Covalent Organometallic Compounds of the Transition Metals," Russ. Chem. Reo. 34, 251-267 (1965); Uspekhi Khim., pp. 585 ff; (m) Rybinskaya, M . I., and Korneva, L. M., "Electrophilic Substitution in Cyclopentadienide Anions," ibid., 40,247-255 (1971); Uspekhi Khim, pp. 444 ff; (n) Leonova, E. V., and Kochetkova, N. S., ibid., 42,278-292 (1973); Uspekhi Khim., pp. 615 ff; (o) Braterman, P. S., and Cross, R. J., "Organo-Transition-metal complexes: Stability, Reactivity and Orbital Correlations," Chem. Soc. Reo., 2, 271 (1973); (p) Hunt, C. B., Educ. Chem., 14,110 (1977). (7) Wilkinson, G., and Cotton, F. A., Chem. Ind., (London), 307 (1954); see also Fischer, E. O., and Hafner, W., Z. Naturforsch., 9b, 503 (1954). (8) Barber, W. A., Inorg. Synth., 6,11 (1960). (9) Hull, H. S., Reid, A. F., and Turnbull, A. G., Inorg. Chem., 6, 805 (1967) and refs. therein. (10) Aleksanyan, V. T., and Lokshin, B. V., J. Organometal. Chem., 131,113 (1977); Alek- sanyan, V. T., Lokshin, B. V., Borisov, G. K., Devyatych, G. G., Nagarova, R. G., Smirnov, A. S., Koningstein, J. A., and Gáchter, B. F-, J. Organometal. Chem., in press. •(11) Weiss, E., and Fisher, E. O., Z. Anorg. Allg. Chem., 278, 219 (1955). (12) Wilkinson, G., Cotton, F. A., and Birmingham, J. M., J. Inorg. Nuclear Chem., 2,95 (1956). (13) Cotton, F. A., and Reynolds, L. J., J. Amer. Chem. Soc, 80, 269 (1958). (14) Lippincott, E. R., Xavier, J., and Steele, D.,J.Amer. Chem. Soc., 83, 2262 (1961). (15) Haaland, A., Lusztyk, J., Novak, D. P., Brunvoll, J., and Starowieyski, K. B., J. Chem. Soc, Chem. Comm., 54 (1974). (16) Haaland, A., Lusztyk, J., Brunvoll, J., and Starowieyski, K. B.,J. Organometal. Chem., 85, 279 (1975). (17) Aleksanyan, V, T., Garbuzova, I. A., Gavrilenko, V. V., and Zakharkin, L. I., J. Or- ganometal. Chem., 129, 139 (1977). lChemical Abstracts nomenclature, from 1974 to the present date for this compound is bis(r) 5 -2,4-cyclopentadien-l-yl)magnesium. In earlier references the compound is variously named: bis(cyclopen- tadienyl)magnesium, (also bis-cyclopentadienylmagnesium), dicy- clopentadienylmagnesium, di-ir-cyclopentadienylmagnesium and magnesium cyclopentadienide. In the present paper, this compound will be referred to by its trivial ñame, magnesocene, for space-saving brevity. 704 / Journal of Chemical Education

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  • A. G. Pinkus Bay lo r Un ive rs i t y

    W a c o , T e x a s 7 6 7 0 3

    Magnesocene: Structure and Bonding

    Covalent or ionic?

    A l t h o u g h t h e m o s t c o m m o n s tate o f c o o r d i n a t i o n for m a g -n e s i u m i n i t s c o m p o u n d s is f o u r (1), examples o f t h r e e - ( 2 ) , f i v e - ( 3 ) , s i x - ( 4 ) , a n d e i g h t - c o o r d i n a t i o n (5) have also been r e p o r t e d . A n u n u s u a l t y p e o f b o n d i n g f o r m a g n e s i u m w h i c h does n o t f i t i n t o a n y o f these categories occurs i n magneso -cene. 1 Magnesocene is a m e m b e r o f t h e genera l class o f o r -g a n o m e t a l l i c c o m p o u n d s k n o w n as meta l locenes (6 ) o r " s a n d w i c h " c o m p o u n d s o f w h i c h t h e f i r s t e x a m p l e t o be rec -ognized is t h e w e l l - k n o w n ferrocene. A l t h o u g h i t is g e n e r a l l y agreed t h a t b o n d i n g i n meta l locenes o f t r a n s i t i o n metis a p -pears t o be p r e d o m i n a n t l y covalent , t h e n a t u r e o f b o n d i n g i n magnesocene is c u r r e n t l y i n d i s p u t e . T h i s p a p e r w i l l p r e s e n t a bref r ev i ew o f t h e s t r u c t u r e s a n d b o n d i n g p r o p o s e d f o r magnesocene l e a d i n g u p t o t h e m o s t r e cent w o r k .

    A l t h o u g h magnesocene was f i r s t p r e p a r e d (7) b y a d d i t i o n o f cyc lopentadiene t o e t h y l m a g n e s i u m b r o m i d e a n d r e m o v i n g e ther so lvent i n vacuo , i t can also be p r e p a r e d (8) b y t h e r e -a c t i o n o f m e t a l l i c m a g n e s i u m w i t h c y c l o p e n t a d i e n e ( e q n . (D) .

    2 C 6 H 6 + M g - H 2 + M g ( C 5 H 5 ) 2 (1) Magnesocene is a use fu l intermedate for t h e p r e p a r a t i o n (9) o f o ther metal locenes e i ther i n t h e m o l t e n state or i n s o l u t i o n (eqn . (2 ) ) . T h e h i g h free energy o f f o r m a t i o n o f M g C l 2 f a v o r s t h e meta thes i s .

    M g ( C 5 H 5 ) 2 + M C 1 2 - M ( C 5 H 5 ) 2 + M g C l 2 (2) Magnesocene has been r e p o r t e d (10) t o have been p r e p a r e d i n a rose-colored m o d i f i c a t i o n i n a d d i t i o n t o the b e t t e r - k n o w n f o r m .

    Weiss a n d F i s h e r (11) d e t e r m i n e d t h a t M g ( C 5 H 5 ) 2 i n t h e c r y s t a l l i n e s tate h a d a s a n d w i c h - l i k e s t r u c t u r e a n d p r o p o s e d weak cova lent d 2 s p 3 h y b r i d i z a t i o n o v e r l a p p i n g t h e i o n i c e lectrostatic b i n d i n g between t h e m e t a l a n d cyc l opentad ieny l ions. Based on magnetic , spectral , a n d chemica l invest igat ions , W i l k i n s o n , C o t t o n , a n d B i r m i n g h a m (12) conc luded t h a t ionic b o n d i n g was present; t h e t w o cyc lopentadienide anions w o u l d be expec ted on e l e c t ros ta t i c g r o u n d s t o a l i g n themse lves o n oppos i t e sides o f t h e cat in w i t h p a r a l l e l p lanes a n d t o v e r y c losely resemble ferrocene . T h e concept o f i o n i c b o n d i n g i n M g ( C s H 5 ) 2 was f u r t h e r e l a b o r a t e d b y C o t t o n a n d R e y n o l d s (13). L i p p i n c o t t , X a v i e r , a n d Steele (14) s t u d i e d t h e i n f r a r e d a n d R a m a n spectra o f s o l u t i o n s a n d t h e s o l i d s tate a n d i n c o m p a r i s o n w i t h s tud ies o n ferrocene c o n f i r m e d t h e s a n d -w i c h - t y p e s t r u c t u r e . H o w e v e r , t h e y c o n c l u d e d t h a t t h e i r r e -su l t s were n o t i n a g r e e m e n t w i t h t h e i on i c b o n d i n g c o n c e p t b u t were b e t t e r e x p l a i n e d b y cova lent r i n g - t o - m e t a l b o n d i n g w h i c h was, however , w e a k e r t h a n t h e m e t a l - t o - r i n g b o n d i n g i n ferrocene . F r o m a gas-phase electrn d i f f r a c t i o n s t u d y , H a a l a n d , et al. (15,16), d e t e r m i n e d t h a t t h e best a g r e e m e n t between calculated a n d e x p e r i m e n t a l intens i t ies was ob ta ined b y assuming ecl ipsed C5H5 r ings (Drt s y m m e t r y ) (see f i g u r e ) . H o w e v e r , a m o d e l w i t h s taggered s y m m e t r y (Z) 5 ( ) c o u l d n o t

    T 2 . 0 0 8

    1 . 4 2 3 A

    Structure of magnesocene (15, 16).

    s i de view ( r i n g s p e r p e n d i c u l a r )

    be conclusively r u l e d o u t . T h e y also conc luded t h a t there was no s ign i f i cant d e v i a t i o n f r o m p l a n a r i t y for the C5H5 r ings a n d t h a t magnesocene is best r e g a r d e d as a cova lent r a t h e r t h a n a n i on i c c o m p o u n d .

    M o r e r e c e n t l y , A l e k s a n y a n a n d coworkers (17) o b t a i n e d R a m a n a n d i n f r a r e d spectra on t h e c o m p o u n d . R a m a n results were f o r so l id a n d m e l t f o r m s a n d i n c l u d e d d e p o l a r i z a t i o n m e a s u r e m e n t s w h i l e i n f r a r e d d a t a f o r t h e s o l i d covered t h e range 400-3200 c m - 1 . T h e i r analys is o f t h e d a t a l ed t o t h e conclus in t h a t t h e M g - C p b o n d is m a i n l y i on i c .

    Literature Cited (1) Bai lar , J . C , Jr. in " T h e Chemistry of the Coordinat ion Compounds," (Editor: Bai lar ,

    J . C , J r . ) , Re inho ld , New Y o r k , 1956, p. 243. (2) For a recent review: P inkus , A. G., Coord. Chem. Rev., 25, 173 (1978). (3) Stucky, G., and Rundle , R. E., J . Amer. Chem. Soc, 86, 4821 (1964); Va l l ino , M . , Or-

    ganometal. Chem., 20, 1 (1969). (4) Schroder, F., and Spandau, H . , Naturwissenschaften, 53, 360 (1966); Schrder, F. A. ,

    Chem. Ber., 102, 2035 (1969); A twood , J . L . , and Stuckey, G. D. , J . Organometal. Chem., 13, 53 (1968); Toney, J . D . , and Stucky , G. D. , J . Organometal Chem., 28, 5 (1971) .

    (5) Shannon, R. D. , and Prewi t t , C. T . , Acta Cryst., B25,925 (1969); Mor t i e r , W. J . , P l u t h , J . J . , and S m i t h , J . B. , Nature, 256, 718 (1975).

    (6) Reviews dealing in p a r t w i t h various aspects of metallocenes (excluding ferrocenes): (a) Pauson, P. L . , " Cyclopentadienyl M e t a l Compounds" in "Organometal l i c Chemis t ry " , (Editor: Zeiss, H . ) , Re inho ld , New Y o r k , 1960, Chap. 7, pp . 346-379; (b) Zeiss, H . , "Arene Complexes o f the T r a n s i t i o n M e t a l s " i n ibid., Chap. 8, pp. 380-425. (c) B irmingham, C. M - , "Synthesis of Cyclopentadienyl M e t a l Compounds," in "Advances in Organometall ic C h e m i s t r y , " Vo l . 2, (Editors : Stone, F . G. A. , and West, R.) Academic Press, New Y o r k , 1964, pp . 365-413; (d) C h u r c h i l l , M . R., and Masn, R., " T h e Structural Chemistry of Organo-Transition Meta l Complexes: Some Recent Developments ," ibid., vo l . 5, 1967, pp. 93-135; (e) Cais, M . , and L u p i n , M . S., "Mass Spectra of Metallocenes & Related Compounds , " ibid., vol . 8, 1970, pp. 211-333; (f) Slocum, D. W., and E r n s t , C. R., "E lec t ron i c Effects in Metallocenes and Certa in Related Systems," ibid., vo l . 10, 1972, pp. 79-114; (g) Bruce , M . I . , "Organo -Trans i t i on M e t a l Chemis t ry -A Guide to the L i t e r a t u r e 1950-1970," ibid., vol . 10, pp. 273-346; (h) Rubezhov, A . Z. and G u b i n , S. P., " L i g a n d S u b s t i t u t i o n in T r a n s i t i o n M e t a l x-Complexes," ibid., vol . 10, pp. 347-417; (i) Bruce, M . I . , " T h e L i terature of Organo-Transit ion M e t a l Chemistry 1971," ibid., vol . 11,1973, pp. 447 ff ; (j) Bruce, M . I . , " T h e L i t e r a t u r e o f Organo T r a n s i t i o n M e t a l Chemistry 1972," ibid., vol . 12, 1974, pp. 379-407; (k) S i l v e r t h o r n , W. E., "Arene T r a n s i t i o n M e t a l Chemis t ry , " i b i d . , vo l . 13, 1975, pp. 47-137; (1) Razuvaev, G. A. , and Latyaeva, V . N . , "Covalent Organometall ic Compounds of the T r a n s i t i o n M e t a l s , " Russ. Chem. Reo. 34, 251-267 (1965); Uspekhi Khim., pp . 585 ff; (m) Rybinskaya, M . I . , and Korneva , L . M . , "E lec t roph i l i c S u b s t i t u t i o n i n Cyclopentadienide An ions , " ibid., 40,247-255 (1971); Uspekhi Khim, pp . 444 ff; (n) Leonova, E. V . , and Kochetkova, N . S., ibid., 42,278-292 (1973); Uspekhi Khim., pp. 615 ff; (o) Braterman , P. S., and Cross, R. J . , "Organo-Trans i t ion-meta l complexes: Stab i l i ty , Reactivity and Orb i ta l Correlations," Chem. Soc. Reo., 2, 271 (1973); (p) H u n t , C. B. , Educ. Chem., 14,110 (1977).

    (7) W i l k i n s o n , G., and Cot ton , F. A. , Chem. Ind., (London) , 307 (1954); see also Fischer, E. O., and Hafner , W., Z. Naturforsch., 9b, 503 (1954).

    (8) Barber, W . A. , Inorg. Synth., 6 ,11 (1960). (9) H u l l , H . S., Reid , A. F., and T u r n b u l l , A . G., Inorg. Chem., 6, 805 (1967) and refs.

    there in . (10) Aleksanyan, V . T . , and Loksh in , B . V . , J . Organometal. Chem., 131,113 (1977); A lek -

    sanyan, V . T . , L o k s h i n , B . V. , Borisov, G. K. , Devyatych , G. G., Nagarova, R. G., Smirnov , A. S., Koningste in , J . A . , and Gchter, B. F-, J . Organometal. Chem., in press.

    (11) Weiss, E., and Fisher, E. O., Z. Anorg. Allg. Chem., 278, 219 (1955). (12) W i l k i n s o n , G., Cot ton , F. A. , and B i r m i n g h a m , J . M . , J . Inorg. Nuclear Chem., 2 ,95

    (1956). (13) Cot ton , F. A., and Reynolds, L . J . , J . Amer. Chem. Soc, 80, 269 (1958). (14) L i p p i n c o t t , E. R., Xavier , J . , and Steele, D.,J.Amer. Chem. Soc., 83, 2262 (1961). (15) Haaland, A., Lusztyk , J . , Novak, D. P., B r u n v o l l , J . , and Starowieyski, K . B. , J . Chem.

    Soc, Chem. Comm., 54 (1974). (16) Haaland, A., Lusztyk , J . , Brunvo l l , J . , and Starowieyski , K . B . , J . Organometal. Chem.,

    85, 279 (1975). (17) Aleksanyan, V , T . , Garbuzova, I . A . , Gavr i lenko , V . V. , and Z a k h a r k i n , L . I . , J . Or-

    ganometal. Chem., 129, 139 (1977).

    lChemical Abstracts nomenclature, from 1974 to the present date for this compound is bis(r) 5-2,4-cyclopentadien-l-yl)magnesium. I n earlier references the compound is variously named: bis(cyclopen-tadienyl)magnesium, (also bis-cyclopentadienylmagnesium), dicy-clopentadienylmagnesium, di-ir-cyclopentadienylmagnesium and magnesium cyclopentadienide. I n the present paper, this compound w i l l be referred to by its t r iv ia l ame, magnesocene, for space-saving brevity.

    7 0 4 / Journal of Chemical Education